Cyclin A and Cdk2 kinase activity are suppressed by combined treatment with tumor necrosis factor-alpha and interferon-alpha

Biochem Biophys Res Commun. 1995 Aug 24;213(3):1115-21. doi: 10.1006/bbrc.1995.2242.

Abstract

We previously reported that combined treatment with tumor necrosis factor-alpha (TNF-alpha) and interferon-alpha (IFN-alpha) showed a synergistic antitumor effect via regulation of cell cycle progression in the S phase. Here, we investigated the effect of the combined treatment with TNF-alpha and IFN-alpha on cell cycle regulating protein in RPMI 4788 cells. Treatment with TNF-alpha or IFN-alpha alone showed no effect on these proteins, however, the combined treatment showed suppression of cyclin A protein and its associated kinase activity. Furthermore, although the combined treatment inhibited Cdk2 kinase activity, the amount of Cdk2 protein was not affected. These results suggested that TNF-alpha and IFN-alpha work together to suppress cyclin A and Cdk2 kinase activity and to inhibit cell cycle progression in the S phase.

MeSH terms

  • CDC2 Protein Kinase / metabolism
  • CDC2-CDC28 Kinases*
  • Colonic Neoplasms / pathology
  • Cyclin-Dependent Kinase 2
  • Cyclin-Dependent Kinases / antagonists & inhibitors*
  • Cyclin-Dependent Kinases / metabolism
  • Cyclins / antagonists & inhibitors*
  • Cyclins / immunology
  • Cyclins / metabolism
  • Drug Interactions
  • Humans
  • Interferon Type I / pharmacology*
  • Precipitin Tests
  • Protamine Kinase / metabolism
  • Protein Serine-Threonine Kinases / antagonists & inhibitors*
  • Protein Serine-Threonine Kinases / metabolism
  • Recombinant Proteins / pharmacology
  • S Phase / drug effects
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Cyclins
  • Interferon Type I
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha
  • Protamine Kinase
  • Protein Serine-Threonine Kinases
  • CDC2 Protein Kinase
  • CDC2-CDC28 Kinases
  • CDK2 protein, human
  • Cyclin-Dependent Kinase 2
  • Cyclin-Dependent Kinases